Thiazol-5-ylmethyl ((2S,5S)-5-amino-1,6-diphenylhexan-2-yl)carbamate hydrochloride

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Reagent Code: #233224
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CAS Number 1370406-80-6

science Other reagents with same CAS 1370406-80-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 446.01 g/mol
Formula C₂₃H₂₈ClN₃O₂S
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors. It plays a role in creating structurally complex molecules that target specific enzymes involved in viral replication, such as those in hepatitis C virus (HCV) treatments. The compound's chiral centers and functional groups allow for precise binding interactions, enhancing drug efficacy and selectivity. Its application is primarily confined to research and development stages in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,580.00
inventory 250mg
10-20 days ฿16,280.00

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Thiazol-5-ylmethyl ((2S,5S)-5-amino-1,6-diphenylhexan-2-yl)carbamate hydrochloride
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors. It plays a role in creating structurally complex molecules that target specific enzymes involved in viral replication, such as those in hepatitis C virus (HCV) treatments. The compound's chiral centers and functional groups allow for precise binding interactions, enhancing drug efficacy and selectivity. Its application is primarily confined to research and development stages in me

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors. It plays a role in creating structurally complex molecules that target specific enzymes involved in viral replication, such as those in hepatitis C virus (HCV) treatments. The compound's chiral centers and functional groups allow for precise binding interactions, enhancing drug efficacy and selectivity. Its application is primarily confined to research and development stages in medicinal chemistry.

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